Does your own blood carry oxygen better than donor blood? a new trial investigates
NCT ID NCT07677150
First seen Jun 30, 2026 · Last updated Jul 01, 2026 · Updated 1 time
Summary
This study looks at how well red blood cells carry oxygen after being processed from a patient's own lost blood during surgery, compared with standard donor blood transfusions. Researchers want to see if the patient's own blood, collected and cleaned by a machine called a cell saver, delivers oxygen more efficiently than stored donor blood. The trial involves adults having major surgery who are likely to need a blood transfusion. Understanding this could help improve how blood is handled before transfusion.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- autologous blood from intraoperative cell salvage
- What this could lead to
- If cell-salvaged blood proves better at delivering oxygen, it could improve patient recovery after major surgery and reduce reliance on donor blood.
- What could go wrong
- This is a small pilot study, so results may not be conclusive. The procedure requires special equipment and may not be suitable for all surgeries.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 418 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Understands and agrees to comply with the study procedures and provides written informed consent as documented by signature. 2. Female and male subjects ≥ 18 years of age at time of consent. 3. Patient undergoes elective surgery according to Surgery List in Protocol Appendix and blood transfusion is likely to happen at the discretion of the investigator. Inclusion criterion 4 only refers to WOCBP 4. Negative urine pregnancy test, not breastfeeding Exclusion Criteria: 1. Known hemoglobinopathy 2. Indication for irradiation of blood products 3. preoperative Anemia (Hb \<11 mg/dl for women and Hb \<12 mg/dl for men) 4. Contraindication for intraoperative cell salvage (septic surgery, tumor surgery) 5. Contraindication for transesophageal Doppler ultrasound (craniofacial dysplasia or fracture, history of esophageal perforation or rupture, esophageal stricture, esophageal varices)
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Medical University Innsbruck
Innsbruck, Tyrol, 6020, Austria
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